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rs1057518087

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518087(C;G)
Make rs1057518087(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position15529699
GeneCYP4F22
is asnp
is mentioned by
dbSNPrs1057518087
dbSNP (old)rs1057518087
ClinGenrs1057518087
ebirs1057518087
HLIrs1057518087
Exacrs1057518087
Gnomadrs1057518087
Varsomers1057518087
Maprs1057518087
PheGenIrs1057518087
Biobankrs1057518087
1000 genomesrs1057518087
hgdprs1057518087
ensemblrs1057518087
gopubmedrs1057518087
geneviewrs1057518087
scholarrs1057518087
googlers1057518087
pharmgkbrs1057518087
gwascentralrs1057518087
openSNPrs1057518087
23andMers1057518087
23andMe allrs1057518087
SNPshotrs1057518087
SNPdbers1057518087
MSV3drs1057518087
GWAS Ctlgrs1057518087
Max Magnitude0
ClinVar
Risk rs1057518087(G;G)
Alt rs1057518087(G;G)
Reference Rs1057518087(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CYP4F22
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.15640510C>G
CLNSRC
CLNACC RCV000414461.1,